http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101658942-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K7-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K7-06 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-095 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-02 |
| filingDate | 2014-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2016-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-101658942-B1 |
| titleOfInvention | Process for the Preparation of Desmopressin |
| abstract | The present invention provides a novel method for preparing desmopressin, which comprises synthesizing a peptide by a solid-phase synthesis method and a solution-phase synthesis method, and then performing a disulfide bond formation reaction in an organic solvent. The present invention performs a solid phase synthesis reaction and a liquid phase reaction, and then performs a disulfide bond formation reaction of the peptide in an organic solvent. Thus, the object can be easily separated and purified after completion of the reaction, so that commercial mass production is possible. In addition, the present invention has improved yield and purity compared to desmopressin synthesized by a method used in the related art, resulting in economical efficiency in terms of production cost. |
| priorityDate | 2014-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 150.